Axplora- The partner of choice for complex APIs.
01 1Axplora
02 1Basic Nutrition
03 1Transo-Pharm Handels GmbH
04 1Moehs Iberica
05 1Pharm-RX Chemical
06 1ZACH System SA
07 1Amara Labs
08 1Arevipharma
09 1Arudavis Labs
10 1Biotechnica DWC
11 1CJ Haide Biotech
12 1F.I.S. Fabbrica Italiana Sintetici
13 1Fujian South Pharmaceutical
14 1Hunan Warrant Chiral Pharmaceutical
15 1Jing Jing Pharmaceutical
16 3Nippon Protein Co Ltd
17 2Nippon Rikagaku Yakuhin
18 1Protchem Industries India Ltd
19 1Seven Star Pharmaceutical
20 1Summit Ingredients
21 1Waitaki Biosciences
22 2Wuhan Grand Hoyo Co
23 1Yangzhou Gami Biochem Co. Ltd
01 1Algeria
02 9China
03 1France
04 3Germany
05 3India
06 1Italy
07 5Japan
08 1New Zealand
09 1Spain
10 1Taiwan
11 1U.S.A
01 6Active
02 2Inactive
03 19Blank
01 1Expired
02 9Valid
03 1Withdrawn by Holder
04 16Blank
01 1217MF10061
02 1218MF10577
03 1219MF10377
04 1220MF10106
05 1224MF10007
06 1224MF10025
07 21Blank
01 27Blank
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-08-07
Pay. Date : 2013-04-03
DMF Number : 5836
Submission : 1985-03-29
Status : Active
Type : II
Certificate Number : R2-CEP 1995-028 - Rev 04
Issue Date : 2020-12-15
Type : Chemical
Substance Number : 967
Status : Valid
Registration Number : 219MF10377
Registrant's Address : ROSENHEIMER STR. 43, D-83064 RAUBLING, GERMARY
Initial Date of Registration : 2007-12-19
Latest Date of Registration :
NDC Package Code : 12598-7027
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Available Reg Filing : EU, CA, BR, CN |
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-22
Pay. Date : 2013-01-07
DMF Number : 14304
Submission : 1999-07-21
Status : Active
Type : II
Certificate Number : R1-CEP 1996-002 - Rev 06
Issue Date : 2021-04-16
Type : Chemical
Substance Number : 967
Status : Valid
NDC Package Code : 52932-0704
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF |
Zach System is committed to providing Highly Customized Solutions for all your Development Programs.
Certificate Number : R1-CEP 2016-311 - Rev 00
Issue Date : 2022-02-07
Type : Chemical
Substance Number : 967
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5091
Submission : 1983-07-04
Status : Active
Type : II
Certificate Number : R1-CEP 1996-070 - Rev 09
Issue Date : 2021-07-23
Type : Chemical
Substance Number : 967
Status : Valid
NDC Package Code : 52133-0002
Start Marketing Date : 1982-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21789
Submission : 2008-07-10
Status : Active
Type : II
Certificate Number : R1-CEP 1998-098 - Rev 02
Issue Date : 2009-05-20
Type : Chemical
Substance Number : 967
Status : Valid
Registration Number : 224MF10025
Registrant's Address : 2-2 Nihonbashi Honcho 4-chome, Chuo-ku, Tokyo
Initial Date of Registration : 2012-02-01
Latest Date of Registration :
NDC Package Code : 52951-001
Start Marketing Date : 1987-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39018
Submission : 2023-12-18
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-09-18
Pay. Date : 2023-07-19
DMF Number : 37947
Submission : 2023-06-26
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7816
Submission : 1988-12-15
Status : Inactive
Type : II
Certificate Number : R1-CEP 1996-080 - Rev 04
Issue Date : 2020-06-19
Type : Chemical
Substance Number : 967
Status : Valid
Registration Number : 224MF10007
Registrant's Address : 575 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2012-01-18
Latest Date of Registration :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3478
Submission : 1979-02-09
Status : Inactive
Type : II
Certificate Number : CEP 2022-177 - Rev 01
Issue Date : 2024-08-01
Type : Chemical
Substance Number : 967
Status : Valid
Registration Number : 220MF10106
Registrant's Address : 575 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2008-04-11
Latest Date of Registration :
Certificate Number : CEP 2010-092 - Rev 03
Issue Date : 2024-06-10
Type : Chemical
Substance Number : 967
Status : Valid
Registrant Name : Daehan New Pharm Co., Ltd.
Registration Date : 2022-08-02
Registration Number : 20110805-139-H-102-03(23)
Manufacturer Name : Wuhan Grand Hoyo Co., Ltd
Manufacturer Address : No.1 Industrial Park, Gedian Economy Development Zone, Hubei, China
Certificate Number : CEP 2022-064 - Rev 01
Issue Date : 2024-06-10
Type : Chemical
Substance Number : 967
Status : Valid
Registrant Name : Daehan New Pharm Co., Ltd.
Registration Date : 2022-08-02
Registration Number : 20110805-139-H-102-03(23)
Manufacturer Name : Wuhan Grand Hoyo Co., Ltd
Manufacturer Address : No.1 Industrial Park, Gedian Economy Development Zone, Hubei, China
Certificate Number : R0-CEP 2002-122 - Rev 01
Issue Date : 2004-11-29
Type : Chemical
Substance Number : 967
Status : Expired
Certificate Number : R1-CEP 2005-018 - Rev 00
Issue Date : 2011-04-20
Type : Chemical
Substance Number : 967
Status : Withdrawn by Holder
Registration Number : 218MF10577
Registrant's Address : 575 Shimada-cho, Ashikaga City, Tochigi Prefecture
Initial Date of Registration : 2006-06-15
Latest Date of Registration :
Registration Number : 217MF10061
Registrant's Address : 4-2-2 Nihonbashi Honcho, Chuo Ward, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration :
NDC Package Code : 52951-001
Start Marketing Date : 1987-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Mucosil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mucosil, including repackagers and relabelers. The FDA regulates Mucosil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mucosil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Mucosil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mucosil supplier is an individual or a company that provides Mucosil active pharmaceutical ingredient (API) or Mucosil finished formulations upon request. The Mucosil suppliers may include Mucosil API manufacturers, exporters, distributors and traders.
click here to find a list of Mucosil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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